Fluorene-containing aromatic compound, material for organic electroluminescent element, and organic electroluminescent element using same

ABSTRACT

A fluorene-containing aromatic compound represented by a formula (1) below. 
     
       
         
         
             
             
         
       
     
     In the formula (1): Nr 1  represents a substituted or unsubstituted monocyclic nitrogen-containing aromatic ring having 2 to 5 ring carbon atoms, or a bicyclic nitrogen-containing aromatic ring having 2 to 9 ring carbon atoms; Ar represents an aromatic ring and the like; Fl 1  and Fl 2  represent a fluorenyl group; and Cz 1  and Cz 2  represent a carbazolyl group. A compound represented by a formula (2) below is omitted from the fluorene-containing aromatic compound represented by the formula (1).

TECHNICAL FIELD

The present invention relates to a fluorene-containing aromaticcompound, a material for an organic electroluminescence device, and anorganic electroluminescence device using the material.

BACKGROUND ART

An organic electroluminescence device (hereinafter, electroluminescenceis occasionally abbreviated as EL) is a self-emitting device based onthe principle that, when an electrical field is applied, a fluorescentmaterial emits light using energy generated by a recombination of holesinjected from an anode with electrons injected from a cathode. Studieson an organic EL device formed of an organic material have beenvigorously carried out since a layered organic EL device driven at lowvoltage was reported (for instance, Patent Literatures 1 to 8). In thelayered device, tris(8-quinolinolato)aluminum is used as an emittinglayer and a triphenyldiamine derivative is used as a hole transportinglayer. Advantages of such a layered structure are to improve efficiencyof injecting holes into the emitting layer, to improve efficiency ofgenerating excitons by recombination due to blockage of electronsinjected from the cathode, to trap the excitons generated in theemitting layer, and the like. As a device structure of such an organicEL device, a two-layered structure, a three-layered structure or thelike has been well known. The two-layered structure includes a holetransporting (injecting) layer and an electron transporting/emittinglayer. The three-layered structure includes a hole transporting(injecting) layer, an emitting layer and an electron transporting(injecting) layer. In such a layered device, a device structure and apreparation method have been contrived in order to improve efficiency ofrecombining the injected holes and electrons.

Luminescent materials of an organic EL device such as a chelate complex(e.g. a tris(8-quinolinol) aluminum complex), a coumarin complex, atetraphenyl butadiene derivative, a distyrylarylene derivative and anoxadiazole derivative have been known. These materials, which have beenreported to emit light of blue to red in visible region, are expected tobe applied to a color-display device.

Moreover, in addition to a fluorescent material, application of aphosphorescent material has been recently proposed for the emittinglayer of the organic EL device. Thus, in the emitting layer of theorganic EL device, a singlet state and a triplet state of excited statesof an organic phosphorescent material are used to achieve a highluminous efficiency. When electrons and holes are recombined in theorganic EL device, it is presumed that a singlet exciton and a tripletexciton are produced at a rate of 1:3 due to difference in spinmultiplicity. Accordingly, luminous efficiency of the device using aphosphorescent material can reach three to four times as much as that ofthe device only using a fluorescent material.

In forming the emitting layer, a doping method, according to which theabove luminescent material (dopant) is doped to a host material, hasbeen known.

The emitting layer formed by the doping method can efficiently generateexcitons from electric charges injected into the host material. With theexciton energy generated by the excitons being transferred to thedopant, the dopant can emit light with high efficiency.

Recently, in order to upgrade an organic EL device, a further study onthe doping method has been made to seek favorable host materials.

Such a host material is disclosed in, for instance, Patent Literatures 1to 6. Patent Literature 1 discloses a compound containing a carbazoleskeleton and a benzimidazole ring in the same molecule, and data of thecompound as a blue fluorescent material host. Patent Literature 2discloses a compound containing a carbazole skeleton and a1,2,4-triazole ring in the same molecule, and data of the compound as ablue to blue-green fluorescent material host. Patent Literature 3discloses a compound containing a carbazole skeleton and animidazopyridine ring in the same molecule, and data of the compound as ablue fluorescent material host. Patent Literature 4 discloses a compoundcontaining a carbazole skeleton, a fluorene skeleton and animidazopyridine ring (a nitrogen-containing aromatic ring) in the samemolecule, and data of the compound as a blue fluorescent material host.Patent Literature 5 discloses a compound containing a carbazole skeletonand a nitrogen-containing aromatic ring in the same molecule, and dataof the compound as a host material used together with a blue toblue-green phosphorescent material. Patent Literature 6 discloses acompound containing a carbazole skeleton, a fluorene skeleton and aphenanthroline ring (a nitrogen-containing aromatic ring) in the samemolecule, and data of the compound as a green phosphorescent materialhost.

Patent Literatures 7 and 8 disclose compounds having the same skeletonsas those of the compounds Patent Literatures 1 to 6. Patent Literature 7discloses a compound containing a carbazole skeleton and a pyridine ringin the same molecule, and data of the compound serving as a holetransporting material. Patent Literature 8 discloses a compoundcontaining a fluorene skeleton and a pyridine ring (anitrogen-containing aromatic ring) in the same molecule, and applicationof the compound to the emitting layer.

CITATION LIST Patent Literatures

Patent Literature 1 JP-A-2001-247858

Patent Literature 2 JP-A-2000-68059

Patent Literature 3 JP-A-2001-192653

Patent Literature 4 US2004-157084

Patent Literature 5 WO2003/080760

Patent Literature 6 WO2004/026870

Patent Literature 7 JP-A-2000-169448

Patent Literature 8 JP-A-2007-261969

SUMMARY OF THE INVENTION Problems to be Solved by the Invention

Although Patent Literatures 1 to 4 disclose data on when the compoundstherein serve as a fluorescent material host, Patent Literatures 1 to 4fail to disclose whether or not the compounds serve as a greenphosphorescent material host. In Patent Literature 5 and 6, in which thecompounds serving as a phosphorescent material host are disclosed,organic EL devices using the compounds do not exhibit a sufficientluminous efficiency and driving voltage for the organic EL devices isnot satisfactory. Patent Literatures 7 and 8 do not disclose whether ornot the compounds therein serve as a phosphorescent material host.

Typically, a phosphorescent organic EL device emits light using excitedtriplet energy. As compared with a typical fluorescent organic ELdevice, a difference in electron affinity between the emitting layer andthe electron transporting layer and a difference in ionization potentialbetween the hole transporting layer and the emitting layer become large,so that carrier injection is blocked to often require high voltage.

An object of the invention is to provide a long-life organic EL devicethat exhibits a high luminous efficiency and is capable of being drivenat low voltage required for power consumption saving and to provide afluorene-containing aromatic compound usable for an organic-EL-devicematerial providing such an organic EL device.

Means for Solving the Problems

After conducting concentrated studies in order to achieve such anobject, the inventors have found that a difference in electron affinitybetween the electron transporting layer and the emitting layer can bereduced by using a material in which a carbazole skeleton and anitrogen-containing hetero aromatic ring are combined, and thatintroduction of a fluorene skeleton in the same molecule improvestransporting performance of carrier (particularly, electrons) andsignificantly lowers voltage applied to a phosphorescent organic ELdevice. In other words, an aromatic compound having a carbazole skeletonrepresented by a formula (1) below, a nitrogen-containing heteroaromatic ring and a fluorene skeleton in the same molecule can beprovided. Also, an organic EL device that can be driven at low voltagerequired for power consumption saving can be provided by using thearomatic compound as an organic-EL-device material.

Specifically, a fluorene-containing aromatic compound represented by theformula (1) according to an aspect of the invention includes a carbazoleskeleton, a nitrogen-containing hetero aromatic ring and a fluoreneskeleton in the same molecule.

In the formula: Nr₁ represents a substituted or unsubstituted monocyclicnitrogen-containing aromatic ring having 2 to 5 carbon atoms for formingthe aromatic ring (hereinafter referred to as ring carbon atoms), or abicyclic nitrogen-containing aromatic ring having 2 to 9 ring carbonatoms; Ar represents a single bond, a substituted or unsubstitutedaromatic ring having 5 to 40 ring carbon atoms; Fl₁ and Fl₂ eachindependently represent a substituted or unsubstituted fluorenyl group;p is an integer of 0 to 3 representing the number of a substituent(s) of-(L₄-Fl₁) directly bonding to Nr₁; when p is 2 or more, L₄ may be thesame or different and Fl₁ may be the same or different; q is an integerof 0 to 3 representing the number of a substituent of -(L₇-Fl₂) directlybonding to Ar; when q is 2 or more, L₇ may be the same or different andFl₂ may be the same or different; p+q=1 or more; Cz₁ and Cz₂ eachindependently represent a substituted or unsubstituted carbazolyl group;m is an integer of 0 to 3 representing the number of a substituent of-(L₂-Cz₁) directly bonding to Nr₁; when m is 2 or more, L₂ may be thesame or different and Cz₁ may be the same or different; n is an integerof 0 to 3 representing the number of a substituent of -(L₅-Cz₂) directlybonding to Ar; when n is 2 or more, L₅ may be the same or different andCz₂ may be the same or different; m+n=1 or more; Y¹ and Y² eachindependently represent a hydrogen atom, a deuterium atom, a fluorineatom, a chlorine atom, a bromine atom, a iodine atom, a cyano group, asubstituted or unsubstituted and linear, branched or cyclic alkyl grouphaving 1 to 20 carbon atoms, a substituted or unsubstituted and linear,branched or cyclic alkoxy group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic haloalkylgroup having 1 to 20 carbon atoms, a substituted or unsubstituted andlinear, branched or cyclic haloalkoxy group having 1 to 20 carbon atoms,a substituted or unsubstituted and linear, branched or cyclic alkylsilylgroup having 1 to 10 carbon atoms, a substituted or unsubstitutedarylsilyl group having 6 to 30 carbon atoms, a substituted orunsubstituted aryl group having 6 to 30 ring carbon atoms, or asubstituted or unsubstituted heteroaryl group having 2 to 10 ring carbonatoms; x is an integer of 1 to 3 representing the number of asubstituent of -(L₃-Y₁) directly bonding to Nr₁; when x is 2 or more, L₃may be the same or different and Y₁ may be the same or different; y isan integer of 1 to 3 representing the number of a substituent of-(L₆-Y₂) directly bonding to Ar; when y is 2 or more, L₆ may be the sameor different and Y₂ may be the same or different; m+p+x is less than orequal to a numeral represented by (the number of the possiblesubstituent(s) for selected Nr₁ minus 1); n+q+y is less than or equal toa numeral represented by (the number of the possible substituent(s) forselected Ar minus 1); and L₁ to L₇ each independently represent a singlebond, a substituted or unsubstituted aromatic ring having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted aromatic heterocyclicring having 2 to 30 ring carbon atoms; and k represents an integer of 1to 3, in which a compound represented by a formula (2) below is omittedfrom the fluorene-containing aromatic compound represented by theformula (1).

In the fluorene-containing aromatic compound according to the aboveaspect of the invention, in the formula (1), Nr₁ is preferably anitrogen-containing aromatic ring selected from a substituted orunsubstituted pyrrole ring, pyrazole ring, imidazole ring, triazolering, pyridine ring, pyrimidine ring, pyridazine ring, pyrazine ring,triazine ring, indole ring, indazole ring, benzimidazole ring, quinolinering, isoquinoline ring, cinnoline ring, quinoxaline ring andimidazopyridine ring.

Moreover, according to the above aspect of the invention, it ispreferable that each of Cz₁ and Cz₂ in the formula (1) is independentlyrepresented by the following formula (3) or (4).

In the formula (3), Ra and Rb each independently represent a hydrogenatom, a deuterium atom, a fluorine atom, a chlorine atom, a bromineatom, a iodine atom, a cyano group, a substituted or unsubstituted andlinear, branched or cyclic alkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic alkoxy grouphaving 1 to 20 carbon atoms, a substituted or unsubstituted and linear,branched or cyclic haloalkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic haloalkoxygroup having 1 to 20 carbon atoms, a substituted or unsubstituted andlinear, branched or cyclic alkylsilyl group having 1 to 10 carbon atoms,a substituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms, a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms; and f and g each independently represent aninteger of 1 to 4.

In the formula (4), Ra′, Rb′ and Rc′ each independently represent ahydrogen atom, a deuterium atom, a fluorine atom, a chlorine atom, abromine atom, a iodine atom, a cyano group, a substituted orunsubstituted and linear, branched or cyclic alkyl group having 1 to 20carbon atoms, a substituted or unsubstituted and linear, branched orcyclic alkoxy group having 1 to 20 carbon atoms, a substituted orunsubstituted and linear, branched or cyclic haloalkyl group having 1 to20 carbon atoms, a substituted or unsubstituted and linear, branched orcyclic haloalkoxy group having 1 to 20 carbon atoms, a substituted orunsubstituted and linear, branched or cyclic alkylsilyl group having 1to 10 carbon atoms, a substituted or unsubstituted arylsilyl grouphaving 6 to 30 carbon atoms, a substituted or unsubstituted aryl grouphaving 6 to 30 ring carbon atoms, or a substituted or unsubstitutedheteroaryl group having 2 to 10 ring carbon atoms; f is an integer of 1to 4; g′ is an integer of 1 to 3; and h′ is an inter of 1 to 5.

According to the above aspect of the invention, in the formula (1), itis preferable that k is 1 and m+n+p+q is less than or equal to 6.

Moreover, it is preferable that each of Y₁ and Y₂ is independentlyrepresented by a hydrogen atom or a phenyl group.

According to the above aspect of the invention, it is preferable that kis 1; L₁, L₂, L₃, L₅ and L₆ each independently represent a single bond,a substituted or unsubstituted phenylene group, a substituted orunsubstituted biphenylene group, a substituted or unsubstitutedterphenylene group, or a substituted or unsubstituted fluorenylenegroup; and L₄ and L₇ each independently represent a single bond, asubstituted or unsubstituted phenylene group, a substituted orunsubstituted biphenylene group, or a substituted or unsubstitutedterphenylene group. When a hydrogen atom is bonded to the above groups,the hydrogen atom may be a deuterium atom.

It is preferable that m+n=1 or 2 and p+q=1 for 2.

Ar is preferably a monocyclic aromatic ring selected from a substitutedor unsubstituted benzene ring, pyrazole ring, imidazole ring, triazolering, pyridine ring, pyrimidine ring, pyridazine ring, pyrazine ring,triazine ring or thiophene ring, particularly preferably a benzene ring.

According to the above aspect of the invention, it is preferable thateach of Fl₁ and Fl₂ in the formula (1) is independently represented by aformula (5) below.

In the formula (5): Y₃ and Y₄ each independently represent: a hydrogenatom; a deuterium atom; a linear, branched or cyclic alkyl group having1 to 10 carbon atoms; a linear, branched or cyclic haloalkyl grouphaving 1 to 10 carbon atoms; a linear, branched or cyclic alkylsilylgroup having 1 to 10 carbon atoms; a substituted or unsubstitutedarylsilyl group having 6 to 30 carbon atoms; a substituted orunsubstituted aryl group having 6 to 30 ring carbon atoms; or asubstituted or unsubstituted heteroaryl group having 2 to 10 ring carbonatoms; and Y₅, Y₆, Y₇, Y₈, Y₉, Y₁₀ and Y₁₁ each independently represent:a hydrogen atom; a deuterium atom; a fluorine atom; a chlorine atom; abromine atom; an iodine atom; a cyano group; a linear, branched orcyclic alkyl group having 1 to 10 carbon atoms; a linear, branched orcyclic alkoxy group having 1 to 10 carbon atoms; a linear, branched orcyclic haloalkyl group having 1 to 10 carbon atoms; a linear, branchedor cyclic haloalkoxy group having 1 to 10 carbon atoms; a linear,branched or cyclic alkylsilyl group having 1 to 10 carbon atoms; asubstituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms; a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms; or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms.

According to the above aspect of the invention, each of Y₃ and Y₄ isindependently a linear alkyl group having 1 to 10 carbon atoms or aphenyl group in the formula (5).

It is more preferable that both of Y₃ and Y₄ are a methyl group.

According to the above aspect of the invention, it is preferable thateach of Cz₁ and Cz₂ in the formula (1) is independently represented by aformula (3) or a formula (4).

According to the aspect of the invention, it is more preferable that Nr₁is a pyrimidine ring in the formula (1).

It is preferable that the fluorene-containing aromatic compound is usedas an organic-electroluminescence-device material.

An organic electroluminescence device according to another aspect of theinvention includes: a cathode; an anode; and an organic thin-film layerprovided between the cathode and the anode, the organic thin-film layerformed out of one or more layers including an emitting layer, in whichat least one layer of the organic thin-film layer contains thefluorene-containing aromatic compound.

In the organic electroluminescence device according to the above aspectof the invention, the emitting layer preferably contains the as a hostmaterial.

It is preferable that the organic electroluminescence device furthercontains a phosphorescent material.

It is more preferable that the emitting layer includes a host materialand a phosphorescent material, in which the phosphorescent material isan ortho metalation of a complex of a metal atom selected from iridium(Ir), osmium (Os) and platinum (Pt).

In the organic electroluminescence device according to the above aspectof the invention, it is preferable that the organic thin-film layerincludes an electron injecting layer provided between the cathode andthe emitting layer, the electron injecting layer containing anitrogen-containing cyclic derivative.

Moreover, it is preferable that the organic thin-film layer includes anelectron transporting layer provided between the cathode and theemitting layer, the electron transporting layer containing thefluorene-containing aromatic compound.

In the organic EL device according to the above aspect of the invention,a reduction-causing dopant is preferably added in an interfacial regionbetween the cathode and the organic thin-film layer.

Effects of the Invention

According to the aspect(s) of the invention, a fluorene-containingcompound represented by the formula (1) is used as an organic-EL-devicematerial to provide an organic EL device with a high luminousefficiency, a long lifetime and low voltage drivability. Moreover, theorganic-EL-device material is effective as an organic-electron-devicematerial for an organic solar cell, an organic semiconductor laser, asensor using an organic substance and an organic TFT.

BRIEF DESCRIPTION OF DRAWING

FIG. 1 schematically shows an exemplary structure of an organicelectroluminescence device according to an exemplary embodiment of theinvention.

DESCRIPTION OF EMBODIMENT

Description will be made below on an exemplary embodiment(s) of theinvention. A fluorene-containing aromatic compound according to thisexemplary embodiment of the invention is suitably used especially as anorganic-EL-device material. The fluorene-containing aromatic compound isused in an organic EL device according to this exemplary embodiment ofthe invention

Structure of Organic EL Device

Firstly, structure(s) of an organic EL device will be described below.

The following are representative structure examples of an organic ELdevice:

-   (1) anode/emitting layer/cathode;-   (2) anode/hole injecting layer/emitting layer/cathode;-   (3) anode/emitting layer/electron injecting·transporting    layer/cathode;-   (4) anode/hole injecting layer/emitting layer/electron    injecting·transporting layer/cathode;-   (5) anode/organic semiconductor layer/emitting layer/cathode;-   (6) anode/organic semiconductor layer/electron blocking    layer/emitting layer/cathode;-   (7) anode/organic semiconductor layer/emitting layer/adhesion    improving layer/cathode;-   (8) anode/hole injecting·transporting layer/emitting layer/electron    injecting·transporting layer/cathode;-   (9) anode/insulating layer/emitting layer/insulating layer/cathode;-   (10) anode/inorganic semiconductor layer/insulating layer/emitting    layer/insulating layer/cathode;-   (11) anode/organic semiconductor layer/insulating layer/emitting    layer/insulating layer/cathode;-   (12) anode/insulating layer/hole injecting·transporting    layer/emitting layer/insulating layer/cathode; and-   (13) anode/insulating layer/hole injecting·transporting    layer/emitting layer/electron injecting·transporting layer/cathode.

The structure (8) is suitably used among the above, but the structure ofthe invention is not limited to the above structures.

FIG. 1 schematically shows an exemplary structure of an organic ELdevice according to an exemplary embodiment of the invention.

The organic EL device 1 includes a transparent substrate 2, an anode 3,a cathode 4 and an organic thin-film layer 10 positioned between theanode 3 and the cathode 4.

The organic thin-film layer 10 includes a phosphorescent-emitting layer5 containing a phosphorescent host as a host material and aphosphorescent dopant as a phosphorescent material. A layer such as ahole injecting/transporting layer 6 may be provided between thephosphorescent-emitting layer 5 and the anode 3 while a layer such as anelectron injecting/transporting layer 7 may be provided between thephosphorescent-emitting layer 5 and the cathode 4.

In addition, an electron blocking layer may be provided to thephosphorescent-emitting layer 5 adjacent to the anode 3 while a holeblocking layer may be provided to the phosphorescent-emitting layer 5adjacent to the cathode 4.

With this structure, electrons and holes can be trapped in thephosphorescent-emitting layer 5, thereby enhancing probability ofexciton generation in the phosphorescent-emitting layer 5.

It should be noted that a “fluorescent host” and a “phosphorescent host”herein respectively mean a fluorescent host combined with a fluorescentdopant and a phosphorescent host combined with a phosphorescent dopant,and that a distinction between the fluorescent host and phosphorescenthost is not unambiguously derived only from a molecular structure of thehost in a limited manner.

In other words, the fluorescent host herein means a material for forminga fluorescent-emitting layer containing a fluorescent dopant, and doesnot mean a host that is only usable as a host of a fluorescent material.

Likewise, the phosphorescent host herein means a material for forming aphosphorescent-emitting layer containing a phosphorescent dopant, anddoes not mean a host that is only usable as a host of a phosphorescentmaterial.

It should be noted that the “hole injecting/transporting layer” hereinmeans “at least either one of a hole injecting layer and a holetransporting layer” while the “electron injecting/transporting layer”herein means “at least either one of an electron injecting layer and anelectron transporting layer.”

Transparent Substrate

The organic EL device according to this exemplary embodiment of theinvention is formed on a light-transmissive substrate. Thelight-transmissive plate, which supports the organic EL device, ispreferably a smooth substrate that transmits 50% or more of light in avisible region of 400 nm to 700 nm.

The light-transmissive plate is exemplarily a glass plate, a polymerplate or the like.

For the glass plate, materials such as soda-lime glass,barium/strontium-containing glass, lead glass, aluminosilicate glass,borosilicate glass, barium borosilicate glass and quartz can be used.

For the polymer plate, materials such as polycarbonate, acryl,polyethylene terephthalate, polyether sulfide and polysulfone can beused.

Anode and Cathode

The anode of the organic EL device is used for injecting holes into thehole injecting layer, the hole transporting layer or the emitting layer.It is effective that the anode has a work function of 4.5 eV or more.

Exemplary materials for the anode are alloys of indium-tin oxide (ITO),tin oxide (NESA), indium zinc oxide, gold, silver, platinum and copper.

The anode may be made by forming a thin film from the above electrodematerials through methods such as vapor deposition and sputtering.

When light from the emitting layer is to be emitted through the anode asin this embodiment, the anode preferably transmits more than 10% of thelight in the visible region. Sheet resistance of the anode is preferablyseveral hundreds Ω/square or lower. Although depending on the materialof the anode, the thickness of the anode is typically in a range of 10nm to 1 μm, and preferably in a range of 10 nm to 200 nm.

The cathode is preferably formed of a material with smaller workfunction in order to inject electrons into the electron injecting layer,the electron transporting layer and the emitting layer.

Although a material for the cathode is subject to no specificlimitation, examples of the material are indium, aluminum, magnesium,alloy of magnesium and indium, alloy of magnesium and aluminum, alloy ofaluminum and lithium, alloy of aluminum, scandium and lithium, and alloyof magnesium and silver.

Like the anode, the cathode may be made by forming a thin film from theabove materials through a method such as vapor deposition or sputtering.In addition, the light may be emitted through the cathode.

Emitting Layer

The emitting layer of the organic EL device has functions as follows.

Specifically:

-   (1) injecting function: a function for accepting, when an electrical    field is applied, the holes injected by the anode or the hole    injecting layer, or the electrons injected by the cathode or the    electron injecting layer;-   (2) transporting function: a function for transporting injected    electric charges (the electrons and the holes) by the force of the    electrical field; and-   (3) emitting function: a function for providing a condition for    recombination of the electrons and the holes to emit light.

Injectability of the holes may differ from that of the electrons andtransporting capabilities of the hole and the electrons (represented bymobilities of the holes and the electrons) may differ from each other.

As a method of forming the emitting layer, known methods such as vapordeposition, spin coating and an LB method may be employed.

The emitting layer is preferably a molecular deposit film.

The molecular deposit film means a thin film formed by depositing amaterial compound in gas phase or a film formed by solidifying amaterial compound in a solution state or in liquid phase. The moleculardeposit film is typically distinguished from a thin film formed by theLB method (molecular accumulation film) by differences in aggregationstructures, higher order structures and functional differences arisingtherefrom.

As disclosed in JP-A-57-51781, the emitting layer can be formed from athin film formed by spin coating or the like, the thin film being formedfrom a solution prepared by dissolving a binder (e.g. a resin) and amaterial compound in a solvent.

The thickness of the emitting layer is preferably in a range of 5 nm to50 nm, more preferably in a range of 7 nm to 50 nm and most preferablyin a range of 10 nm to 50 nm. The thickness less than 5 nm may causedifficulty in forming the emitting layer and in controllingchromaticity, while the thickness more than 50 nm may increase drivingvoltage.

The organic EL device according to this exemplary embodiment includes: acathode; an anode; and a single or a plurality of organic thin-filmlayers provided between the cathode and the anode, in which the organicthin-film layer(s) includes at least one emitting layer, and the organicthin-film layer(s) includes at least one phosphorescent material and atleast one organic-EL-device material according to another aspect of theinvention (later described). In addition, at least one of the emittinglayer(s) preferably contains the organic-EL-device material of theexemplary embodiment and at least one phosphorescent material.

Organic-EL-Device Material

The organic-EL-device material according to this exemplary embodiment isrepresented by a formula (1) below.

In the formula (1): Nr₁ represents a substituted or unsubstitutedmonocyclic nitrogen-containing aromatic ring having 2 to 5 ring carbonatoms, or a bicyclic nitrogen-containing aromatic ring having 2 to 9ring carbon atoms; Ar represents a single bond, a substituted orunsubstituted aromatic ring having 5 to 40 ring carbon atoms; Fl₁ andFl₂ each independently represent a substituted or unsubstitutedfluorenyl group; p is an integer of 0 to 3 representing the number of asubstituent of -(L₄-Fl₁) directly bonding to Nr₁; when p is 2 or more,L₄ may be the same or different and Fl₁ may be the same or different; qis an integer of 0 to 3 representing the number of a substituent of-(L₇-Fl₂) directly bonding to Ar; when q is 2 or more, L₇ may be thesame or different and Fl₂ may be the same or different; p+q=1 or more;Cz₁ and Cz₂ each independently represent a substituted or unsubstitutedcarbazolyl group; m is an integer of 0 to 3 representing the number of asubstituent of -(L₂-Cz₁) directly bonding to Nr₁; when m is 2 or more,L₂ may be the same or different and Cz₁ may be the same or different; nis an integer of 0 to 3 representing the number of a substituent of-(L₅-Cz₂) directly bonding to Ar; when n is 2 or more, L₅ may be thesame or different and Cz₂ may be the same or different; m+n=1 or more;Y¹ and Y² each independently represent a hydrogen atom, a deuteriumatom, a fluorine atom, a chlorine atom, a bromine atom, a iodine atom, acyano group, a substituted or unsubstituted and linear, branched orcyclic alkyl group having 1 to 20 carbon atoms, a substituted orunsubstituted and linear, branched or cyclic alkoxy group having 1 to 20carbon atoms, a substituted or unsubstituted and linear, branched orcyclic haloalkyl group having 1 to 20 carbon atoms, a substituted orunsubstituted and linear, branched or cyclic haloalkoxy group having 1to 20 carbon atoms, a substituted or unsubstituted and linear, branchedor cyclic alkylsilyl group having 1 to 10 carbon atoms, a substituted orunsubstituted arylsilyl group having 6 to 30 carbon atoms, a substitutedor unsubstituted aryl group having 6 to 30 ring carbon atoms, or asubstituted or unsubstituted heteroaryl group having 2 to 10 ring carbonatoms; x is an integer of 1 to 3 representing the number of asubstituent of -(L₃-Y₁) directly bonding to Nr₁; when x is 2 or more, L₃may be the same or different and Y₁ may be the same or different; y isan integer of 1 to 3 representing the number of a substituent of-(L₆-Y₂) directly bonding to Ar; when y is 2 or more, L₆ may be the sameor different and Y₂ may be the same or different; m+p+x is less than orequal to a numeral represented by (the number of the possiblesubstituent(s) for selected Nr₁ minus 1); n+q+y is less than or equal toa numeral represented by (the number of the possible substituent(s) forselected Ar minus 1); and L₁ to L₇ each independently represent a singlebond, a substituted or unsubstituted aromatic ring having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted aromatic heterocyclicring having 2 to 30 ring carbon atoms; and k represents an integer of 1to 3, in which a compound represented by the following formula (2) isomitted from the organic-EL-device material represented by the formula(1).

In the formula (1), Nr₁ is preferably a nitrogen-containing aromaticring selected from a substituted or unsubstituted pyrrole ring, pyrazolering, imidazole ring, triazole ring, pyridine ring, pyrimidine ring,pyridazine ring, pyrazine ring, triazine ring, indole ring, indazolering, benzimidazole ring, quinoline ring, isoquinoline ring, cinnolinering, quinoxaline ring and imidazopyridine ring. When a hydrogen atom isbonded to the nitrogen-containing aromatic ring, the hydrogen atom maybe a deuterium atom.

Nr₁ is more preferably a substituted or unsubstituted pyridine ring,pyrimidine ring, or triazine ring, particularly preferably a substitutedor unsubstituted pyrimidine ring. In the formula (1), when Nr₁ is animidazopyridine ring, a case where both of Y₃ and Y₄ in Fl₂ are a phenylgroup may be omitted.

Moreover, in the formula (1), when Nr₁ is an imidazopyridine ring, acase where L₇ is a single bond may be omitted.

In the formula (1), Ar is preferably a monocyclic aromatic ring such asa substituted or unsubstituted benzene ring having 2 to 6 ring carbonatoms, pyrazole ring, imidazole ring, triazole ring, pyridine ring,pyrimidine ring, pyridazine ring, pyrazine ring, triazine ring orthiophene ring, particularly preferably a benzene ring. When a hydrogenatom is bonded to the monocyclic aromatic ring, the hydrogen atom may bea deuterium atom.

In addition, preferably, each of Cz₁ and Cz₂ in the formula (1) isindependently represented by the following formula (3) or (4).

In the formula, Ra and Rb each independently represent a hydrogen atom,a deuterium atom, a fluorine atom, a chlorine atom, a bromine atom, aiodine atom, a cyano group, a substituted or unsubstituted and linear,branched or cyclic alkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic alkoxy grouphaving 1 to 20 carbon atoms, a substituted or unsubstituted and linear,branched or cyclic haloalkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic haloalkoxygroup having 1 to 20 carbon atoms, a substituted or unsubstituted andlinear, branched or cyclic alkylsilyl group having 1 to 10 carbon atoms,a substituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms, a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms; and f and g each independently represent aninteger of 1 to 4.

In the formula, Ra′, Rb′ and Rc′ each independently represent a hydrogenatom, a deuterium atom, a fluorine atom, a chlorine atom, a bromineatom, a iodine atom, a cyano group, a substituted or unsubstituted andlinear, branched or cyclic alkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic alkoxy grouphaving 1 to 20 carbon atoms, a substituted or unsubstituted and linear,branched or cyclic haloalkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic haloalkoxygroup having 1 to 20 carbon atoms, a substituted or unsubstituted andlinear, branched or cyclic alkylsilyl group having 1 to 10 carbon atoms,a substituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms, a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms; f′ is an integer of 1 to 4; g′ is an integerof 1 to 3; and h′ is an inter of 1 to 5.

In addition, preferably, each of Cz₁ and Cz₂ is independentlyrepresented by the following formula (3a) or (4a).

In the formula (1), it is preferable that k is 1 and m+n+p+q is lessthan or equal to 6. More preferably, m+n=1 or 2 and p+q=______ or 2. mrepresents the number of a substituent(s) of -(L₂-Cz₁) directly bondingto Nr₁. Likewise, n, p and q represent the number of a substituent(s).

In the formula (1), preferably, Y₁ and Y₂ each independently represent ahydrogen atom, a substituted or unsubstituted aryl group having 6 to 30ring carbon atoms or a substituted or unsubstituted heteroaryl grouphaving 2 to 10 ring carbon atoms, particularly preferably a hydrogenatom or a phenyl group.

In the formula (1), it is preferable that L₁, L₂, L₃, L₅ and L₆ eachindependently represent a single bond, a substituted or unsubstitutedphenylene group, a substituted or unsubstituted biphenylene group, asubstituted or unsubstituted terphenylene group, or a substituted orunsubstituted fluorenylene group; and L₄ and L₇ each independentlyrepresent a single bond, a substituted or unsubstituted phenylene group,a substituted or unsubstituted biphenylene group, or a substituted orunsubstituted terphenylene group. When a hydrogen atom is bonded to theabove groups, the hydrogen atom may be a deuterium atom.

In the formula (1), preferably, each of Fl₁ and Fl₂ is independentlyrepresented by the following formula (5).

In the formula (5): Y₃ and Y₄ each independently represent: a hydrogenatom; a deuterium atom; a linear, branched or cyclic alkyl group having1 to 10 carbon atoms; a linear, branched or cyclic haloalkyl grouphaving 1 to 10 carbon atoms; a linear, branched or cyclic alkylsilylgroup having 1 to 10 carbon atoms; a substituted or unsubstitutedarylsilyl group having 6 to 30 carbon atoms; a substituted orunsubstituted aryl group having 6 to 30 ring carbon atoms; or asubstituted or unsubstituted heteroaryl group having 2 to 10 ring carbonatoms; and Y₅, Y₆, Y₇, Y₈, Y₉, Y₁₀ and Y₁₁ each independently represent:a hydrogen atom; a deuterium atom; a fluorine atom; a chlorine atom; abromine atom; an iodine atom; a cyano group; a linear, branched orcyclic alkyl group having 1 to 10 carbon atoms; a linear, branched orcyclic alkoxy group having 1 to 10 carbon atoms; a linear, branched orcyclic haloalkyl group having 1 to 10 carbon atoms; a linear, branchedor cyclic haloalkoxy group having 1 to 10 carbon atoms; a linear,branched or cyclic alkylsilyl group having 1 to 10 carbon atoms; asubstituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms; a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms; or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms.

Further, in the formula (5), Y₃ and Y₄ each independently represent alinear, branched or cyclic alkyl group having 1 to 10 carbon atoms, alinear, branched or cyclic alkylsilyl group having 1 to 10 carbon atomsor a phenyl group. Y₅, Y₆, Y₇, Y₈, Y₉, Y₁₀ and Y₁₁ are preferably ahydrogen atom. More preferably, Y₃ and Y₄ each are independently alinear alkyl group having 1 to 10 carbon atoms or a phenyl group. Amongthe above, particularly preferably, Y₃ and Y₄ each are represented by amethyl group.

When Nr₁, Ar, Y₁, Y₂, Fl₁, Fl₂, Cz₁, Cz₂, and L₁ to L₇ in the formulae(1) and (3) to (5) each have one substituent or a plurality ofsubstituents, the substituent(s) is preferably a linear, branched orcyclic alkyl group having 1 to 20 carbon atoms, a haloalkyl group having1 to 20 carbon atoms, a linear, branched or cyclic alkylsilyl grouphaving 1 to 10 carbon atoms, a cyano group, a halogen atom, or an arylgroup having 6 to 22 ring carbon atoms.

Examples of the linear, branched or cyclic alkyl group having 1 to 20carbon atoms are a methyl group, ethyl group, propyl group, isopropylgroup, n-butyl group, s-butyl group, isobutyl group, t-butyl group,n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonylgroup, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecylgroup, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group,n-heptadecyl group, n-octadecyl group, neo-pentyl group, 1-methylpentylgroup, 2-methylpentyl group, 1-pentylhexyl group, 1-butylpentyl group,1-heptyloctyl group, 3-methylpentyl group, cyclopentyl group, cyclohexylgroup, cyclooctyl group and 3,5-tetramethylcyclohexyl group.

Examples of the linear, branched or cyclic alkylsilyl group having 1 to10 carbon atoms are a trimethylsilyl group, triethylsilyl group,tributylsilyl group, dimethylethylsilyl group, dimethylisopropylsilylgroup, dimethylpropylsilyl group, dimethylbutylsilyl group,dimethyl-tertiary-butylsilyl group and diethylisopropylsilyl group.

Examples of the arylsilyl group having 6 to 30 carbon atoms are aphenyldimethylsilyl group, diphenylmethylsilyl group,diphenyl-tertiary-butylsilyl group and triphenylsilyl group.

Examples of the halogen atom are a fluorine atom, a chlorine atom, abromine atom and an iodine atom.

Examples of the aryl group having 6 to 30 ring carbon atoms are a phenylgroup, biphenyl group, terphenyl group, naphthyl group, fluoranthenylgroup, triphenylenyl group and phenanthrenyl group.

Examples of the heteroaryl group having 2 to 10 ring carbon atoms are apyrrolyl group, pyrazinyl group, pyridinyl group, indolyl group,isoindolyl group, furyl group, benzofuranyl group, isobenzofuranylgroup, dibenzofuranyl group, dibenzothiophenyl group, quinolyl group,isoquinolyl group, quinoxalinyl group, carbazolyl group, phenanthridinylgroup, acridinyl group, phenanthrolinyl group and thienyl group.

Examples of the aromatic ring having 6 to 30 ring carbon atoms are abenzene ring, naphthalene ring, phenanthrene ring, biphenyl ring,terphenyl ring and quarter-phenyl ring.

Examples of the aromatic heterocyclic group having 2 to 30 ring carbonatoms are a pyridine ring, pyrazine ring, pyrimidine ring, pyridazinering, triazine ring, indole ring, quinoline ring, acridine ring,pyrrolidine ring, dioxane ring, piperidine ring, morpholine ring,piperazine ring, carbazole ring, furan ring, thiophene ring, oxazolering, oxadiazole ring, benzoxazole ring, thiazole ring, thiadiazolering, benzothiazole ring, triazole ring, imidazole ring, benzimidazolering, pyrane ring and dibenzofuran ring.

Examples of the fluorene-containing aromatic compound according to thisexemplary embodiment represented by the formula (1) are as follows.

In the organic EL device according to this exemplary embodiment, theemitting layer preferably contains the fluorene-containing aromaticcompound as a host material. In addition, the emitting layer ispreferably formed of a host material and a phosphorescent material whilethe host material is the fluorene-containing aromatic compound.

The fluorene-containing aromatic compound may be a host material usedwith a phosphorescent material, or may be an electron transportingmaterial used with a phosphorescent material. The fluorene-containingaromatic compound preferably has an excited triplet energy of 2.2 eV to3.2 eV, more preferably 2.4 eV to 3.2 eV.

The organic EL device according to this exemplary embodiment maypreferably include an electron transporting layer that contains theorganic-EL-device material according to this exemplary embodiment.

The organic EL device according to this exemplary embodiment maypreferably include at least one of the electron transporting layer andthe hole blocking layer that contains the organic-EL-device materialaccording to this exemplary embodiment.

The organic EL device according to this exemplary embodiment maypreferably include the hole transporting layer (hole injecting layer)that contains the organic-EL-device material according to this exemplaryembodiment.

Phosphorescent Material

According to this exemplary embodiment, the phosphorescent materialpreferably contains a metal complex, and the metal complex preferablyhas a metal atom selected from Ir, Pt, Os, Au, Cu, Re and Ru, and aligand. Particularly, the ligand preferably has an ortho-metal bond.

The phosphorescent material is preferably a compound containing a metalselected from iridium (Ir), osmium (Os) and platinum (Pt) because such acompound, which exhibits high phosphorescence quantum yield, can furtherenhance external quantum efficiency of the emitting device. Thephosphorescent material is more preferably a metal complex such as aniridium complex, osmium complex or platinum complex, among which aniridium complex and platinum complex are more preferable and orthometalation of an iridium complex is the most preferable.

Examples of such a preferable metal complex are shown below.

According to this exemplary embodiment, at least one of thephosphorescent material contained in the emitting layer preferably emitslight with the maximum wavelength of 450 nm to 720 nm.

By doping the phosphorescent material (phosphorescent dopant) havingsuch an emission wavelength to the specific host material used in thisexemplary embodiment to form the emitting layer, the organic EL devicecan exhibit high efficiency.

Reduction-Causing Dopant

In the organic EL device according to this exemplary embodiment, areductive dopant may be preferably contained in an interfacial regionbetween the cathode and the organic thin-film layer.

With this structure, the organic EL device can emit light with enhancedluminance intensity and have a longer lifetime.

The reduction-causing dopant may be at least one compound selected froma group of an alkali metal, alkali metal complex, alkali metal compound,alkali earth metal, alkali earth metal complex, alkali earth metalcomplex compound, rare-earth metal, rare-earth metal complex, arare-earth metal compound and the like.

Examples of the alkali metal are Na (work function: 2.36 eV), K (workfunction: 2.28 eV), Rb (work function: 2.16 eV), and Cs (work function:1.95 eV), among which the alkali metal having a work function of 2.9 eVor less is particularly preferable. Among the above, thereduction-causing dopant is preferably K, Rb or Cs, more preferably Rbor Cs, the most preferably Cs.

Examples of the alkali earth metal are Ca (work function: 2.9 eV), Sr(work function: 2.0 eV to 2.5 eV), and Ba (work function: 2.52 eV),among which the alkali earth metal having a work function of 2.9 eV orless is particularly preferable.

Examples of the rare-earth metal are Sc, Y, Ce, Tb, and Yb, among whichthe rare-earth metal having a work function of 2.9 eV or less isparticularly preferable.

Since the above preferred metals have particularly high reducibility,addition of a relatively small amount of the metals to an electroninjecting zone can enhance luminance intensity and lifetime of theorganic EL device.

Examples of the alkali metal compound are an alkali oxide such as Li₂O,Cs₂O or K₂O, and an alkali halogen compound such as LiF, NaF, CsF or KF,among which LiF, Li₂O and NaF are preferable.

Examples of the alkali earth metal compound are BaO, SrO, CaO, and amixture thereof such as Ba_(x)Sr_(1-x)O (0<x<1) or Ba_(x)Ca_(1-x)O(0<x<1), among which BaO, SrO and CaO are preferable.

Examples of the rare-earth metal compound are YbF₃, ScF₃, ScO₃, Y₂O₃,Ce₂O₃, GdF₃, TbF₃ and the like, among which YbF₃, ScF₃ and TbF₃ arepreferable.

The alkali metal complex, alkali earth metal complex and rare-earthmetal complex are subject to no limitation as long as they contain atleast one metal ion of an alkali metal ion, an alkali earth metal ionand a rare-earth metal ion. The ligand is preferably quinolinol,benzoquinolinol, acridinol, phenanthridinol, hydroxyphenyl oxazole,hydroxyphenyl thiazole, hydroxydiaryl oxadiazole, hydroxydiarylthiadiazole, hydroxyphenyl pyridine, hydroxyphenyl benzoimidazole,hydroxybenzo triazole, hydroxy fluborane, bipyridyl, phenanthroline,phthalocyanine, porphyrin, cyclopentadiene, β-diketones, azomethines, ora derivative thereof, but the ligand is not limited thereto.

The reduction-causing dopant is added to preferably form a layer or anisland pattern in the interfacial region. The layer of thereduction-causing dopant or the island pattern of the reduction-causingdopant is preferably formed by depositing the reduction-causing dopantby resistance heating deposition while an emitting material for formingthe interfacial region or an organic substance as an electron-injectingmaterial are simultaneously deposited, so that the reduction-causingdopant is dispersed in the organic substance. Dispersion concentrationat which the reduction-causing dopant is dispersed in the organicsubstance is a mole ratio (organic substance to reduction-causingdopant) of 100:1 to 1:100, preferably 5:1 to 1:5.

When the reduction-causing dopant forms the layer, the emitting materialor the electron injecting material for forming the organic layer of theinterfacial region is initially layered, and the reduction-causingdopant is subsequently deposited singularly thereon by resistanceheating deposition to form a preferably 0.1 nm- to 15 nm-thick layer.

When the reduction-causing dopant forms the island pattern, the emittingmaterial or the electron injecting material for forming the organiclayer of the interfacial region is initially formed in an island shape,and the reduction-causing dopant is subsequently deposited singularlythereon by resistance heating deposition to form a preferably 0.05 nm-to 1 nm-thick island shape.

A ratio of the main component to the reduction-causing dopant in theorganic EL device according to this exemplary embodiment is preferably amole ratio (main component to reductive dopant) of 5:1 to 1:5, morepreferably 2:1 to 1:2.

Electron Injecting Layer and Electron Transporting Layer

The electron injecting layer or the electron transporting layer, whichaids injection of the electrons into the emitting layer, has a largeelectron mobility. The electron injecting layer is provided foradjusting energy level, by which, for instance, sudden changes in theenergy level can be reduced.

The organic EL device according to this exemplary embodiment preferablyincludes the electron injecting layer between the emitting layer and thecathode, and the electron injecting layer preferably contains anitrogen-containing cyclic derivative as a main component. The electroninjecting layer may serve as an electron transporting layer.

It should be noted that “as a main component” means that thenitrogen-containing cyclic derivative is contained in the electroninjecting layer at a content of 50 mass % or more.

A preferable example of an electron transporting material for formingthe electron injecting layer is an aromatic heterocyclic compound havingat least one heteroatom in a molecule. Particularly, anitrogen-containing cyclic derivative is preferable. Thenitrogen-containing cyclic derivative is preferably an aromatic ringhaving a nitrogen-containing six-membered or five-membered ringskeleton, or a fused aromatic cyclic compound having anitrogen-containing six-membered or five-membered ring skeleton.

The nitrogen-containing cyclic derivative is preferably exemplified by anitrogen-containing cyclic metal chelate complex represented by thefollowing formula (A).

R² to R⁷ in the formula (A) each independently represent a hydrogenatom, halogen atom, oxy group, amino group, hydrocarbon group having 1to 40 carbon atoms, alkoxy group, aryloxy group, alkoxycarbonyl group,or heterocyclic group. These groups may be substituted or unsubstituted.

Examples of the halogen atom include fluorine, chlorine, bromine, andiodine. In addition, examples of the substituted or unsubstituted aminogroup include an alkylamino group, an arylamino group, and anaralkylamino group.

The alkoxycarbonyl group is represented by —COOY′. Examples of Y′ arethe same as the examples of the alkyl group. The alkylamino group andthe aralkylamino group are represented by —NQ¹Q². Examples for each ofQ¹ and Q² are the same as the examples described in relation to thealkyl group and the aralkyl group, and preferred examples for each of Q¹and Q² are also the same as those described in relation to the alkylgroup and the aralkyl group. Either one of Q¹ and Q² may be a hydrogenatom.

The arylamino group is represented by —NAr¹Ar². Examples for each of Ar¹and Ar² are the same as the examples described in relation to thenon-fused aryl group and the fused aryl group. Either one of Ar¹ and Ar²may be a hydrogen atom.

M represents aluminum (Al), gallium (Ga) or indium (In), among which Inis preferable.

L in the formula (A) represents a group represented by a formula (A′) or(A″) below.

In the formula (A′), R⁸ to R¹² each independently represent a hydrogenatom or a substituted or unsubstituted hydrocarbon group having 1 to 40carbon atoms. Adjacent groups may form a cyclic structure. In theformula (A″), R¹³ to R²⁷ each independently represent a hydrogen atom ora substituted or unsubstituted hydrocarbon group having 1 to 40 carbonatoms. Adjacent groups may form a cyclic structure.

Examples of the hydrocarbon group having 1 to 40 carbon atomsrepresented by each of R⁸ to R¹² and R¹³ to R²⁷ in the formulae (A′) and(A″) are the same as those of R² to R⁷.

Examples of a divalent group formed when an adjacent set of R⁸ to R¹²and R¹³ to R²⁷ forms a cyclic structure are a tetramethylene group, apentamethylene group, a hexamethylene group, a diphenylmethane-2,2′-diylgroup, a diphenylethane-3,3′-diyl group, and a diphenylpropane-4,4′-diylgroup.

In the exemplary embodiment of the invention, the aromatic compoundrepresented by the formulae (1) and (3) to (5) is preferably containedas the electron transporting layer.

As an electron transporting compound for the electron injecting layer orthe electron transporting layer, 8-hydroxyquinoline or a metal complexof its derivative, an oxadiazole derivative, and a nitrogen-containingheterocyclic derivative are preferable. A specific example of the8-hydroxyquinoline or the metal complex of its derivative is a metalchelate oxinoid compound containing a chelate of oxine (typically8-quinolinol or 8-hydroxyquinoline). For instance, tris(8-quinolinol)aluminum can be used. Examples of the oxadiazole derivative are asfollows.

In the formula, Ar¹⁷, Ar¹⁸, Ar¹⁹, Ar²¹, Ar²² and Ar²⁵ each represent asubstituted or unsubstituted aryl group. Ar¹⁷, Ar¹⁹ and Ar²² may be thesame as or different from Ar¹⁸, Ar²¹ and Ar²⁵ respectively. Ar²⁰, Ar²³and Ar²⁴ each represent a substituted or unsubstituted arylene group.Ar²³ and Ar²⁴ may be mutually the same or different.

Examples of the arylene group are a phenylene group, naphthylene group,biphenylene group, anthranylene group, perylenylene group and pyrenylenegroup. Examples of the substituent therefor are an alkyl group having 1to 10 carbon atoms, alkoxy group having 1 to 10 carbon atoms and cyanogroup.

Such an electron transporting compound is preferably an electrontransporting compound that can be favorably formed into a thin film(s).Examples of the electron transporting compound are as follows.

An example of the nitrogen-containing heterocyclic derivative as theelectron transporting compound is a nitrogen-containing compound that isnot a metal complex, the derivative being formed of an organic compoundrepresented by one of the following general formulae. Examples of thenitrogen-containing heterocyclic derivative are a five-membered ring orsix-membered ring derivative having a skeleton represented by thefollowing formula (A) and a derivative having a structure represented bythe following formula (B).

In the formula (B), X represents a carbon atom or a nitrogen atom. Z₁and Z₂ each independently represent an atom group from which anitrogen-containing heterocycle can be formed.

Preferably, the nitrogen-containing heterocyclic derivative is anorganic compound having a nitrogen-containing aromatic polycyclic grouphaving a five-membered ring or six-membered ring. Further, when thenitrogen-containing heterocyclic derivative is such anitrogen-containing aromatic polycyclic group that contains pluralnitrogen atoms, the nitrogen-containing heterocyclic derivative ispreferably a nitrogen-containing aromatic polycyclic organic compoundhaving a skeleton formed by a combination of the skeletons respectivelyrepresented by the formulae (A) and (B), or by a combination of theskeletons respectively represented by the formulae (A) and (C).

A nitrogen-containing group of the nitrogen-containing aromaticpolycyclic organic compound is selected from nitrogen-containingheterocyclic groups respectively represented by the following generalformulae.

the formulae: R represents an aryl group having 6 to 40 carbon atoms,heteroaryl group having 3 to 40 carbon atoms, alkyl group having 1 to 20carbon atoms or alkoxy group having 1 to 20 carbon atoms; and nrepresents an integer in a range of 0 to 5. When n is an integer of 2 ormore, plural R may be mutually the same or different.

A preferable specific compound is a nitrogen-containing heterocyclicderivative represented by the following formula.

HAr-L¹-Ar¹—Ar²

In the formula: HAr represents a substituted or unsubstitutednitrogen-containing heterocycle having 3 to 40 carbon atoms; L¹represents a single bond, substituted or unsubstituted arylene grouphaving 6 to 40 carbon atoms, or substituted or unsubstitutedheteroarylene group having 3 to 40 carbon atoms; Ar¹ represents asubstituted or unsubstituted divalent aromatic hydrocarbon group having6 to 40 carbon atoms; and Ar^(e) represents a substituted orunsubstituted aryl group having 6 to 40 carbon atoms, or substituted orunsubstituted heteroaryl group having 3 to 40 carbon atoms.

HAr is exemplarily selected from the following group.

L¹ is exemplarily selected from the following group.

Ar¹ is exemplarily selected from the following arylanthranil group.

In the formula: R¹ to R¹⁴ each independently represent a hydrogen atom,halogen atom, alkyl group having 1 to 20 carbon atoms, alkoxy grouphaving 1 to 20 carbon atoms, aryloxy group having 6 to 40 carbon atoms,substituted or unsubstituted aryl group having 6 to 40 carbon atoms, orheteroaryl group having 3 to 40 carbon atoms; and Ar³ represents asubstituted or unsubstituted aryl group having 6 to 40 carbon atoms, ora heteroaryl group having 3 to 40 carbon atoms.

All of R¹ to R⁸ of a nitrogen-containing heterocyclic derivative may behydrogen atoms.

Ar² is exemplarily selected from the following group.

Other than the above, the following compound (see JP-A-9-3448) can befavorably used for the nitrogen-containing aromatic polycyclic organiccompound as the electron transporting compound.

In the formula: R₁ to R₄ each independently represent a hydrogen atom,substituted or unsubstituted aliphatic group, substituted orunsubstituted alicyclic group, substituted or unsubstituted carbocyclicaromatic cyclic group, or substituted or unsubstituted heterocyclicgroup; and X₁ and X₂ each independently represent an oxygen atom, sulfuratom or dicyanomethylene group.

The following compound (see JP-A-2000-173774) can also be favorably usedfor the electron transporting compound.

In the formula, R¹, R², R³ and R⁴, which may be mutually the same ordifferent, each represent an aryl group represented by the followingformula.

In the formula, R⁵, R⁶, R⁷, R⁸ and R⁹, which may be mutually the same ordifferent, each represent a hydrogen atom, saturated or unsaturatedalkoxy group, alkyl group, amino group or alkylamino group. At least oneof R⁵, R⁶, R⁷, R⁸ and R⁹ represents a saturated or unsaturated alkoxygroup, alkyl group, amino group or alkylamino group.

A polymer compound containing the nitrogen-containing heterocyclic groupor a nitrogen-containing heterocyclic derivative may be used for theelectron transporting compound.

The electron transporting layer preferably contains at least one ofnitrogen-containing heterocycle derivatives respectively represented bythe following formulae (201) to (203).

In the formulae (201) to (203), R represents a hydrogen atom,substituted or unsubstituted aryl group having 6 to 60 carbon atoms,substituted or unsubstituted pyridyl group, substituted or unsubstitutedquinolyl group, substituted or unsubstituted alkyl group having 1 to 20carbon atoms, or substituted or unsubstituted alkoxy group having 1 to20 carbon atoms. n represents an integer of 0 to 4. R¹ represents asubstituted or unsubstituted aryl group having 6 to 60 carbon atoms,substituted or unsubstituted pyridyl group, substituted or unsubstitutedquinolyl group, substituted or unsubstituted alkyl group having 1 to 20carbon atoms, or alkoxy group having 1 to 20 carbon atoms. R² and R³each independently represent a hydrogen atom, substituted orunsubstituted aryl group having 6 to 60 carbon atoms, substituted orunsubstituted pyridyl group, substituted or unsubstituted quinolylgroup, substituted or unsubstituted alkyl group having 1 to 20 carbonatoms, or substituted or unsubstituted alkoxy group having 1 to 20carbon atoms. L represents a substituted or unsubstituted arylene grouphaving 6 to 60 carbon atoms, substituted or unsubstituted pyridinylenegroup, substituted or unsubstituted quinolinylene group, or substitutedor unsubstituted fluorenylene group. Ar¹ represents a substituted orunsubstituted arylene group having 6 to 60 carbon atoms, substituted orunsubstituted pyridinylene group, or substituted or unsubstitutedquinolinylene group. Ar² represents substituted or unsubstituted arylgroup having 6 to 60 carbon atoms, substituted or unsubstituted pyridylgroup, substituted or unsubstituted quinolyl group, substituted orunsubstituted alkyl group having 1 to 20 carbon atoms, or substituted orunsubstituted alkoxy group having 1 to 20 carbon atoms.

Ar³ represents a substituted or unsubstituted aryl group having 6 to 60carbon atoms, substituted or unsubstituted pyridyl group, substituted orunsubstituted quinolyl group, substituted or unsubstituted alkyl grouphaving 1 to 20 carbon atoms, substituted or unsubstituted alkoxy grouphaving 1 to 20 carbon atoms or a group represented by —Ar¹—Ar² (Ar¹ andAr² may be the same as the above).

In the formulae (201) to (203), R represents a hydrogen atom,substituted or unsubstituted aryl group having 6 to 60 carbon atoms,substituted or unsubstituted pyridyl group, substituted or unsubstitutedquinolyl group, substituted or unsubstituted alkyl group having 1 to 20carbon atoms, or substituted or unsubstituted alkoxy group having 1 to20 carbon atoms.

Although a thickness of the electron injecting layer or the electrontransporting layer is subject to no limitation, the thickness ispreferably 1 nm to 100 nm.

The electron injecting layer preferably contains an inorganic compoundsuch as an insulator or a semiconductor in addition to thenitrogen-containing cyclic derivative. Such an insulator or asemiconductor, when contained in the electron injecting layer, caneffectively prevent a current leak, thereby enhancing electroninjectability.

As the insulator, it is preferable to use at least one metal compoundselected from the group consisting of an alkali metal chalcogenide, analkali earth metal chalcogenide, a halogenide of alkali metal and ahalogenide of alkali earth metal. When the electron injecting layer isformed from the alkali metal chalcogenide or the like, the electroninjectability can preferably be further enhanced. Specifically,preferred examples of the alkali metal chalcogenide are Li₂O, K₂O, Na₂S,Na₂Se and Na₂O, while preferable example of the alkali earth metalchalcogenide are CaO, BaO, SrO, BeO, BaS and CaSe. Preferred examples ofthe halogenide of the alkali metal are LiF, NaF, KF, LiCl, KCl and NaCl.Preferred examples of the halogenide of the alkali earth metal arefluorides such as CaF₂, BaF₂, SrF₂, MgF₂ and BeF₂, and halogenides otherthan the fluoride.

Examples of the semiconductor are one of or a combination of two or moreof an oxide, a nitride or an oxidized nitride containing at least oneelement selected from Ba, Ca, Sr, Yb, Al, Ga, In, Li, Na, Cd, Mg, Si,Ta, Sb and Zn. An inorganic compound for forming the electron injectinglayer is preferably a microcrystalline or amorphous insulative film.When the electron injecting layer is formed of such insulative film,more uniform thin film can be formed, thereby reducing pixel defectssuch as a dark spot. Examples of such an inorganic compound are thealkali metal chalcogenide, alkali earth metal chalcogenide, halogenideof the alkali metal and halogenide of the alkali earth metal.

When the electron injecting layer contains such an insulator orsemiconductor, a thickness thereof is preferably in a range ofapproximately 0.1 nm to 15 nm. The electron injecting layer according tothis exemplary embodiment may preferably contain the above-describedreduction-causing dopant.

Hole Injecting Layer and Hole Transporting Layer

The hole injecting layer or the hole transporting layer (including thehole injecting/transporting layer) may contain an aromatic aminecompound such as an aromatic amine derivative represented by thefollowing formula (I).

In the formula (I), Ar¹ to Ar⁴ each represent a substituted orunsubstituted aryl group having 6 to 50 ring carbon atoms, substitutedor unsubstituted heteroaryl group having 5 to 50 atoms for forming aring, or a group formed by bonding the aryl group to the heteroarylgroup.

Examples of the compound represented by the formula (I) are shown below.However, the compound represented by the formula (I) is not limitedthereto.

Aromatic amine represented by the following (II) can also be preferablyused for forming the hole injecting layer or the hole transportinglayer.

In the above (II), Ar¹ to Ar³ each represent the same as Ar¹ to Ar⁴ ofthe above formula (I). Examples of the compound represented by thegeneral formula (II) are shown below. However, the compound representedby the formula (II) is not limited thereto.

It should be noted that the invention is not limited to the abovedescription but may include any modification as long as suchmodification stays within a scope and a spirit of the present invention.

For instance, the following is a preferable example of such modificationmade to the invention.

According to this exemplary embodiment, the emitting layer may alsopreferably contain an assistance substance for assisting injection ofcharges.

When the emitting layer is formed of a host material having a wideenergy gap, a difference in ionization potential (Ip) between the hostmaterial and the hole injecting/transporting layer etc. becomes so largethat injection of the holes into the emitting layer becomes difficult,which may cause a rise in a driving voltage required for providingsufficient luminance.

In the above instance, introducing a hole-injectable orhole-transportable assistance substance for assisting injection ofcharges in the emitting layer can contribute to facilitation of theinjection of the holes into the emitting layer and to reduction of thedriving voltage.

As the assistance substance for assisting the injection of charges, forinstance, a general hole injecting material, a general hole transportingmaterial or the like can be used.

Examples of the assistance substance are a triazole derivative (see, forinstance, the specification of U.S. Pat. No. 3,112,197), an oxadiazolederivative (see, for instance, the specification of U.S. Pat. No.3,189,447), an imidazole derivative (see, for instance, JP-B-37-16096),a polyarylalkane derivative (see, for instance, the specifications ofU.S. Pat. No. 3,615,402, No. 3,820,989, and No. 3,542,544, JP-B-45-555,JP-B-51-10983, JP-A-51-93224, JP-A-55-17105, JP-A-56-4148,JP-A-55-108667, JP-A-55-156953 and JP-A-56-36656), a pyrazolinederivative and a pyrazolone derivative (see, for instance, thespecifications of U.S. Pat. No. 3,180,729 and No. 4,278,746,JP-A-55-88064, JP-A-55-88065, JP-49-105537, JP-A-55-51086,JP-A-56-80051, JP-A-56-88141, JP-A-57-45545, JP-A-54-112637 andJP-A-55-74546), a phenylenediamine derivative (see, for instance, thespecification of U.S. Pat. No. 3,615,404, JP-B-51-10105, JP-B-46-3712,JP-B-47-25336, JP-A-54-53435, JP-A-54-110536 and JP-A-54-119925), anarylamine derivative (see, for instance, the specifications of U.S. Pat.No. 3,567,450, No. 3,180,703, No. 3,240,597, No. 3,658,520, No.4,232,103, No. 4,175,961 and No. 4,012,376, JP-B-49-35702,JP-B-39-27577, JP-A-55-144250, JP-A-56-119132 and JP-A-56-22437 and thespecification of West Germany Patent No. 1,110,518), anamino-substituted chalcone derivative (see, for instance, thespecification of U.S. Pat. No. 3,526,501), an oxazole derivative(disclosed in, for instance, the specification of U.S. Pat. No.3,257,203), a styrylanthracene derivative (see, for instance,JP-A-56-46234), a fluorenone derivative (see, for instance,JP-A-54-110837), a hydrazone derivative (see, for instance, thespecification of U.S. Pat. No. 3,717,462 and JP-A-54-59143,JP-A-55-52063, JP-A-55-52064, JP-A-55-46760, JP-A-55-85495,JP-A-57-11350, JP-A-57-148749 and JP-A-02-311591), a stilbene derivative(see, for instance, JP-A-61-210363, JP-A-61-228451, JP-A-61-14642,JP-A-61-72255, JP-A-62-47646, JP-A-62-36674, JP-A-62-10652,JP-A-62-30255, JP-A-60-93455, JP-A-60-94462, JP-A-60-174749 andJP-A-60-175052), a silazane derivative (see the specification of U.S.Pat. No. 4,950,950), a polysilane type (see JP-A-02-204996), ananiline-based copolymer (see JP-A-02-282263), and a conductive polymeroligomer (particularly, thiophene oligomer) disclosed in JP-A-01-211399.

The hole-injectable material, examples of which are as listed above, ispreferably a porphyrin compound (disclosed in JP-A-63-295695 etc.), anaromatic tertiary amine compound or a styrylamine compound (see, forinstance, the specification of U.S. Pat. No. 4,127,412, JP-A-53-27033,JP-A-54-58445, JP-A-54-149634, JP-A-54-64299, JP-A-55-79450,JP-A-55-144250, JP-A-56-119132, JP-A-61-295558, JP-A-61-98353 orJP-A-63-295695), particularly preferably an aromatic tertiary aminecompound.

In addition, 4,4′-bis(N-(1-naphthyl)-N-phenylamino)biphenyl(hereinafter, abbreviated as NPD) having two fused aromatic rings in themolecule as disclosed in U.S. Pat. No. 5,061,569, or4,4′,4″tris(N-(3-methylphenyl)-N-phenylamino)triphenylamine(hereinafter, abbreviated as MTDATA) in which three triphenylamine unitsare bonded in a starburst form as disclosed in JP-A-04-308688 and thelike may also be used.

Further, a hexaazatriphenylene derivative disclosed in Japanese PatentNo. 3614405 and No. 3571977 and U.S. Pat. No. 4,780,536 may alsopreferably be used as the hole-injectable material.

Alternatively, inorganic compounds such as p-type Si and p-type SiC canalso be used as the hole-injecting material.

A method of forming each of the layers in the organic EL deviceaccording to the aspect of the invention is not particularly limited. Aconventionally-known method such as vacuum deposition or spin coatingmay be employed for forming the layers. The organic thin-film layercontaining the compound represented by the formula (1), which is used inthe organic EL device according to the exemplary embodiment of theinvention, may be formed by a conventional coating method such as vacuumdeposition, molecular beam epitaxy (MBE method) and coating methodsusing a solution such as a dipping, spin coating, casting, bar coating,and roll coating.

Although the thickness of each organic layer of the organic EL device isnot particularly limited, the thickness is generally preferably in arange of several nanometers to 1 μm because an excessively-thinned filmlikely entails defects such as a pin hole while an excessively-thickenedfilm requires high voltage to be applied and deteriorates efficiency.

EXAMPLES

Next, the invention will be described in further detail by exemplifyingExample(s) and Comparative(s). However, the invention is not limited bythe description of Example(s).

Synthesis Example 1 Synthesis of Compound No. 1

Under an Ar gas atmosphere, 2,4,6-trichloropyrimidine (18.3 g, 100mmol), phenylboronic acid (24.4 g, 200 mmol), palladium acetate (0.56 g,2.5 mmol), triphenylphosphine (1.31 g, 5.0 mmol), DME (930 ml) and anaqueous solution of 2M sodium carbonate (310 ml) were stirred for 15hours at a reflux temperature. The solvent was distilled away underreduced pressure. The obtained residue was extracted by dichloromethane.The residue obtained by concentrating the organic phase was refined bysilica-gel column chromatography (a developing solvent: hexane-ethylacetate) to provide an intermediate body X₁ as a white solid. A yield ofthe intermediate body X₁ was 18.7 g and a yield rate thereof was 70%.(reference document: J. Org. Chem. 66 7125-7128 (2001))

Under an Ar gas atmosphere, N-(3,5-dibromophenyl)carbazole (12.2 g, 30.4mmol), 9,9-dimethylfluorene-2-boronic acid (7.24 g, 30.4 mmol), anaqueous solution of 2M sodium carbonate (30 ml), toluene (60 ml), DME(30 ml) and Pd(PPh₃)₄ (1.75 g) were stirred for 7 hours at a refluxtemperature. After the reactant solution was cooled down to the roomtemperature, toluene (200 ml) and water (100 ml) were added thereto toseparate an organic phase. The residue obtained by concentrating theorganic phase was refined by silica-gel column chromatography (adeveloping solvent: hexane-toluene) to provide an intermediate body X₂as a white solid. A yield of the intermediate body X₂ was 9.4 g and ayield rate thereof was 60%.

The intermediate body X₂ (5.14 g, 10 mmol) was added in dehydrated THF(100 ml), and was stirred at −70 degrees C. under an Ar gas atmosphere.Next, n-BuLi (1.6M in hexane) (6.3 ml) was dropped thereinto. Afterstirring for two hours at −70 degrees C., 5.64 g (30 mmol) oftriisopropylborate was dropped thereinto. After stirring for one hour at−70 degrees C., the reactant mixture was stirred at the room temperaturefor five hours. Subsequently, 1N-hydrochloric acid (30 ml) was addedthereto and stirred for one hour at the room temperature. THF wasdistilled away under reduced pressure and was extracted bydichloromethane to provide an organic phase. The organic phase was driedby anhydrous magnesium sulfate. The residue obtained by concentratingthe solvent was washed with toluene to provide an intermediate body X₃as a white solid. A yield of the intermediate body X₃ was 3.1 g and ayield rate thereof was 65%.

Under an Ar gas atmosphere, the intermediate body X₃ (4.8 g, 10 mmol),the intermediate body X₁ (2.66 g, 10 mmol), an aqueous solution of 2Msodium carbonate (12 ml), toluene (20 ml), DME (20 ml) and Pd(PPh₃)₄(0.35 g) were stirred for 16 hours at a reflux temperature. After thereactant solution was cooled down to the room temperature, toluene (200ml) and water (100 ml) were added thereto to separate an organic phase.The residue obtained by concentrating the organic phase was refined bysilica-gel column chromatography (a developing solvent: hexane-toluene)and was recrystallized by toluene twice to provide a target object (acompound No. 1) as a white solid. A yield of the compound No. 1 was 3.0g and a yield rate thereof was 45%.

FD mass analysis consequently showed that m/e was equal to 665 while acalculated molecular weight was 654.

Synthesis Example 2 Synthesis of Compound No. 2

Under an Ar gas atmosphere, 2,4,6-trichloropyrimidine (25.0 g, 136.3mmol), phenylboronic acid (16.6 g, 136.3 mmol), palladium acetate(1.53g, 6.82 mmol), triphenylphosphine (3.58 g, 13.6 mmol), DME (1250ml) and an aqueous solution of 2M sodium carbonate (211 ml) were stirredfor 16 hours at a reflux temperature. The solvent was distilled awayunder reduced pressure. The obtained residue was extracted bydichloromethane. The residue obtained by concentrating the organic phasewas refined by silica-gel column chromatography (a developing solvent:hexane-ethyl acetate) to provide an intermediate body X₄ as a whitesolid. A yield of the intermediate body X₄ was 22.1 g and a yield ratethereof was 72%. (reference document: J. Org. Chem. 66 7125-7128 (2001))

Under an Ar gas atmosphere, 2,4-dichloro-6-phenylpyrimidine (theintermediate body X₄) (6.0 g, 26.6 mmol), 9,9-dimethylfluorene-2-boronicacid (6.34 g, 26.6 mmol), palladium acetate (0.30 g, 1.33 mmol),triphenylphosphine (0.70 g, 2.66 mmol), DME (250 ml) and an aqueoussolution of 2M sodium carbonate (42 ml) were stirred for 8 hours at areflux temperature. The solvent was distilled away under reducedpressure. The obtained residue was extracted by toluene. The residueobtained by concentrating the organic phase was refined by silica-gelcolumn chromatography (a developing solvent: hexane-toluene) to providean intermediate body X₅ as a white solid. A yield of the intermediatebody X₅ was 7.2 g and a yield rate thereof was 70%.

Under an Ar gas atmosphere, 3,5-bis-carbazolylphenyl boronic acid(4.52g, 10 mmol), the intermediate body X₅ (3.83 g, 10 mmol), an aqueoussolution of 2M sodium carbonate (12 ml), toluene (20 ml), DME (20 ml)and Pd(PPh₃)₄ (0.35 g) were stirred for 16 hours at a refluxtemperature. After the reactant solution was cooled down to the roomtemperature, toluene (200 ml) and water (100 ml) were added thereto toseparate an organic phase. The residue obtained by concentrating theorganic phase was refined by silica-gel column chromatography (adeveloping solvent: hexane-toluene) and was recrystallized by toluenetwice to provide a target object (a compound No. 2) as a white solid. Ayield of the compound No. 2 was 3.0 g and a yield rate thereof was 40%.

FD mass analysis consequently showed that m/e was equal to 754 while acalculated molecular weight was 754.

Synthesis Example 3 Synthesis of Compound No. 3

3-bromobenzaldehyde (18.5 g, 100 mmol), acetophenone (12.0 g, 100 mmol),1N-sodium methoxide/methanol solution (10 ml) and ethanol (200 ml) werestirred for five hours at the room temperature under an Ar gasatmosphere. Subsequently, the reactant mixture was heated and stirredfor another four hours at a reflux temperature. Next, benzamidinehydrochloride (9.4 g, 60 mmol) and sodium hydroxide (8.0 g, 200 mmol)were added thereto and stirred for five hours at 70 degrees C. After thereaction, the reactant mixture was filtered to separate an extract. Theextract was refined by silica-gel column chromatography (a developingsolvent: dichloromethane) to provide an intermediate body X₆ as a whitesolid. A yield of the intermediate body X₆ was 10.1 g and a yield ratethereof was 26%.

Under an Ar gas atmosphere, the intermediate body X₃ (4.8 g, 10 mmol),the intermediate body X₆ (3.9 g, 10 mmol), an aqueous solution of 2Msodium carbonate (12 ml), toluene (20 ml), DME (20 ml) and Pd(PPh₃)₄(0.35 g) were stirred for 16 hours at a reflux temperature. After thereactant solution was cooled down to the room temperature, toluene (200ml) and water (100 ml) were added thereto to separate an organic phase.The residue obtained by concentrating the organic phase was refined bysilica-gel column chromatography (a developing solvent: hexane-toluene)and was recrystallized by toluene twice to provide a target object (acompound No. 3) as a white solid. A yield of the compound No. 3 was 3.2g and a yield rate thereof was 43%.

FD mass analysis consequently showed that m/e was equal to 741 while acalculated molecular weight was 741.

Synthesis Example 4 Synthesis of Compound No. 4

4-bromobenzaldehyde (18.5 g, 100 mmol), acetophenone (12.0 g, 100 mmol),1N-sodium methoxide/methanol solution (10 ml) and ethanol (200 ml) werestirred at room temperature for 5 hours at the room temperature under anAr gas atmosphere. Subsequently, the reactant mixture was heated andstirred for another four hours at a reflux temperature. Next,benzamidine hydrochloride (9.4 g, 60 mmol) and sodium hydroxide (8.0 g,200 mmol) were added thereto and stirred for five hours at 70 degrees C.After the reaction, the reactant mixture was filtered to separate anextract. The extract was refined by silica-gel column chromatography (adeveloping solvent: dichloromethane) to provide an intermediate body X₇as a white solid. A yield of the intermediate body X₇ was 11.6 g and ayield rate thereof was 30%.

Under an Ar gas atmosphere, the intermediate body X₃ (4.8 g, 10 mmol),the intermediate body X₇ (3.9 g, 10 mmol), an aqueous solution of 2Msodium carbonate (12 ml), toluene (20 ml), DME (20 ml) and Pd(PPh₃)₄(0.35 g) were stirred for 16 hours at a reflux temperature. After thereactant solution was cooled down to the room temperature, toluene (200ml) and water (100 ml) were added thereto to separate an organic phase.The residue obtained by concentrating the organic phase was refined bysilica-gel column chromatography (a developing solvent: hexane-toluene)and was recrystallized by toluene twice to provide a target object (acompound No. 4) as a white solid. A yield of the compound No. 4 was 2.6g and a yield rate thereof was 35%.

FD mass analysis consequently showed that m/e was equal to 741 while acalculated molecular weight was 741.

Synthesis Example 5 Synthesis of Compound No. 5

Under an Ar gas atmosphere, the intermediate body X₅ (3.8 g, 10 mmol),4-carbazolylphenyl boronic acid (2.9 g, 10 mmol), an aqueous solution of2M sodium carbonate (12 ml), toluene (20 ml), DME (20 ml) and Pd(PPh₃)₄(0.35 g) were stirred for 20 hours at a reflux temperature. After thereactant solution was cooled down to the room temperature, toluene (200ml) and water (100 ml) were added thereto to separate an organic phase.The residue obtained by concentrating the organic phase was refined bysilica-gel column chromatography (a developing solvent: hexane-toluene)and was recrystallized by toluene twice to provide a target object (acompound No. 5) as a white solid. A yield of the compound No. 5 was 2.8g and a yield rate thereof was 47%.

FD mass analysis consequently showed that m/e was equal to 589 while acalculated molecular weight was 589.

Example 1 Manufacture of Organic EL Device 1

A glass substrate (size: 25 mm×75 mm×1.1 mm) having an ITO transparentelectrode (manufactured by Geomatec Co., Ltd.) was ultrasonic-cleaned inisopropyl alcohol for five minutes, and then UV(Ultraviolet)/ozone-cleaned for 30 minutes.

After the glass substrate having the transparent electrode was cleaned,the glass substrate was mounted on a substrate holder of a vacuumdeposition apparatus, and a hole injecting layer was initially formed bydepositing a compound A onto the substrate to be 40 nm thick to cover asurface of the glass substrate where a transparent electrode line wasprovided. Next, a compound B was deposited onto the hole injecting layerto be 20 nm thick to provide a hole transporting layer.

On the hole transporting layer, the compound No. 1 as a phosphorescenthost and Ir(Ph-ppy)₃ as a phosphorescent dopant were co-evaporated(thickness: 40 nm), thereby providing a phosphorescent-emitting layer.The concentration of Ir(Ph-ppy)₃ was 20 mass %.

On the phosphorescent-emitting layer, a 30-nm thick film of a compoundC, a 1-nm thick film of LiF, an 80-nm thick film of a metal Al werelaminated in sequence, thereby providing a cathode. LiF, which is anelectron injectable electrode, was formed at a speed of 1 Å/min.

Evaluation on Luminescent Performance of Organic EL Device

The organic EL devices each manufactured as described above were drivenby direct-current electricity to emit light, so that luminance intensityand current density were measured to obtain voltage and luminousefficiency at a current density of 1 mA/cm². Further, time elapsed untilthe initial luminance intensity of 20,000 cd/m² was reduced to the half(i.e., time until half-life) was obtained. The results are shown inTable 1.

Examples 2 to 5

The organic EL devices according respectively to Examples 2 to 5 wereformed and evaluated in the same manner as in Example 1 except that thehost compound No. 1 was replaced by host materials described in Table 1.The results of the evaluation are shown in Table 1.

Comparative 1

An organic EL device according to Comparative 1 was formed and evaluatedin the same manner as in Example 1 except that the host compound No. 1was replaced by a compound D (a host material described inWO2003/08076). The results of the evaluation are shown in Table 1.

TABLE 1 Luminous Time until efficiency half-life Host Voltage (V) (cd/A)(hrs) compound @1 mA/cm² @1 mA/cm² 20000 cd/m² Example 1 No. 1 3.2 86.7350 Example 2 No. 2 3.0 87.9 450 Example 3 No. 3 3.6 88.3 500 Example 4No. 4 3.5 81.3 500 Example 5 No. 5 3.1 74.4 300 Comparative Compound D4.7 51.1 300 1

As seen from Table 1, the organic EL devices of Examples were emittableat low voltage and exhibited a high luminous efficiency as compared withthe organic EL device of Comparative 1.

Example 6

A glass substrate (size: 25 mm×75 mm×1.1 mm) having an ITO transparentelectrode (manufactured by Geomatec Co., Ltd.) was ultrasonic-cleaned inisopropyl alcohol for five minutes, and then UV(Ultraviolet)/ozone-cleaned for 30 minutes.

After the glass substrate having the transparent electrode was cleaned,the glass substrate was mounted on a substrate holder of a vacuumdeposition apparatus, and a hole injecting layer was initially formed bydepositing a compound A onto the substrate to be 40 nm thick to cover asurface of the glass substrate where a transparent electrode line wasprovided. Next, a compound B was deposited onto the hole injecting layerto be 20 nm thick to provide a hole transporting layer.

On the hole transporting layer, the compound D as a phosphorescent hostand Ir(Ph-ppy)₃ as a phosphorescent dopant were co-evaporated(thickness: 40 nm), thereby providing a phosphorescent-emitting layer.The concentration of Ir(Ph-ppy)₃ was 20 mass %.

On the phosphorescent-emitting layer, a 5-nm thick film of the compoundNo.2, a 25-nm thick film of the compound C, a 1-nm thick film of LiF, an80-nm thick film of a metal Al were laminated in sequence, therebyproviding a cathode. LiF, which is an electron injectable electrode, wasformed at a speed of 1 Å/min.

The results of the evaluation of the organic EL device are shown inTable 2. The comparative 1 shown in Table 2 as a comparative is the sameas the comparative 1 above.

TABLE 2 Time until Luminous half- Voltage efficiency life Electron (V)(cd/A) (hrs) Host transporting @1 @1 20000 compound compound mA/cm²mA/cm² cd/m² Example 6 Compound No. 2 4.7 52.5 400 D ComparativeCompound none 4.7 51.1 300 1 D

As seen from Table 2, the compound of the invention was usable as anelectron transporting compound and the organic EL devices of Exampleshad a longer lifetime than the organic EL device of the comparative.

As described in detail, when the compounds of the invention are used asan organic-EL-device material, an organic EL device having a highluminous efficiency and being emittable at low voltage is obtainable.Accordingly, the organic EL device of the invention is significantlyusable as a light source of various electronic devices and the like.Moreover, the compound of the invention is effectively usable as anorganic-electron-device material for an organic solar cell, an organicsemiconductor laser, a sensor using an organic substance and an organicTFT.

INDUSTRIAL APPLICABILITY

The invention is applicable to a long-life organic EL device thatexhibits a high luminous efficiency and is capable of being driven atlow voltage required for power consumption saving as well as to anorganic-EL-device material providing such an organic EL device.

EXPLANATION OF CODES

1 organic electroluminescence device

2 substrate

3 anode

4 cathode

5 phosphorescent-emitting layer

6 hole injecting/transporting layer

7 electron injecting/transporting layer

10 organic thin-film layer

1. A fluorene-containing aromatic compound represented by formula (1):

wherein: Nr₁ represents a substituted or unsubstituted monocyclicnitrogen-containing aromatic ring having 2 to 5 ring carbon atoms, or abicyclic nitrogen-containing aromatic ring having 2 to 9 ring carbonatoms; Ar represents a single bond, a substituted or unsubstitutedaromatic ring having 5 to 40 ring carbon atoms; Fl₁ and Fl₂ eachindependently represent a substituted or unsubstituted fluorenyl group;p represents an integer of 0 to 3, such that when p is 2 or more, L₄ isthe same or different and Fl₁ is the same or different; q represents aninteger of 0 to 3, such that when q is 2 or more, L₇ is the same ordifferent and Fl₂ is the same or different; p+q=1 or more; Cz₁ and Cz₂each independently represent a substituted or unsubstituted carbazolylgroup; m represents an integer of 0 to 3, such that when m is 2 or more,L₂ is the same or different and Cz₁ is the same or different; nrepresents an integer of 0 to 3, such that when n is 2 or more, L₅ isthe same or different and Cz₂ is the same or different; m+n=1 or more;Y¹ and Y² each independently represent a hydrogen atom, a deuteriumatom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom,a cyano group, a substituted or unsubstituted and linear, branched orcyclic alkyl group having 1 to 20 carbon atoms, a substituted orunsubstituted and linear, branched or cyclic alkoxy group having 1 to 20carbon atoms, a substituted or unsubstituted and linear, branched orcyclic haloalkyl group having 1 to 20 carbon atoms, a substituted orunsubstituted and linear, branched or cyclic haloalkoxy group having 1to 20 carbon atoms, a substituted or unsubstituted and linear, branchedor cyclic alkylsilyl group having 1 to 10 carbon atoms, a substituted orunsubstituted arylsilyl group having 6 to 30 carbon atoms, a substitutedor unsubstituted aryl group having 6 to 30 ring carbon atoms, or asubstituted or unsubstituted heteroaryl group having 2 to 10 ring carbonatoms; x represents an integer of 1 to 3, such that when x is 2 or more,L₃ is the same or different and Y₁ is the same or different; yrepresents an integer of 1 to 3, such that when y is 2 or more, L₆ isthe same or different and Y₂ is the same or different; m+p+x is lessthan or equal to the number of substituents of Nr₁ minus 1; n+q+y isless than or equal to the number of substituents of Ar minus 1; L₁ to L₇each independently represent a single bond, a substituted orunsubstituted aromatic ring having 6 to 30 ring carbon atoms, or asubstituted or unsubstituted aromatic heterocyclic ring having 2 to 30ring carbon atoms; k is an integer of 1 to 3; and thefluorene-containing aromatic compound represented by formula (1) is nota compound represented by formula (2):


2. The compound of claim 1, wherein Nr₁ is a nitrogen-containingaromatic ring selected from the group consisting of a substituted orunsubstituted pyrrole ring, a pyrazole ring, an imidazole ring, atriazole ring, a pyridine ring, a pyrimidine ring, a pyridazine ring, apyrazine ring, a triazine ring, an indole ring, an indazole ring, abenzimidazole ring, a quinoline ring, an isoquinoline ring, a cinnolinering, a quinoxaline ring and an imidazopyridine ring.
 3. The compound ofclaim 1, wherein: Cz¹ to Cz³ are independently represented by formula(3) or formula (4):

wherein: Ra and Rb each independently represent a hydrogen atom, adeuterium atom, a fluorine atom, a chlorine atom, a bromine atom, aniodine atom, a cyano group, a substituted or unsubstituted and linear,branched or cyclic alkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic alkoxy grouphaving 1 to 20 carbon atoms, a substituted or unsubstituted and linear,branched or cyclic haloalkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic haloalkoxygroup having 1 to 20 carbon atoms, a substituted or unsubstituted andlinear, branched or cyclic alkylsilyl group having 1 to 10 carbon atoms,a substituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms, a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms; f and g independently represent an integer of1 to 4,

wherein: Ra′, Rb′ and Rc′ each independently represent a hydrogen atom,a deuterium atom, a fluorine atom, a chlorine atom, a bromine atom, aniodine atom, a cyano group, a substituted or unsubstituted and linear,branched or cyclic alkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic alkoxy grouphaving 1 to 20 carbon atoms, a substituted or unsubstituted and linear,branched or cyclic haloalkyl group having 1 to 20 carbon atoms, asubstituted or unsubstituted and linear, branched or cyclic haloalkoxygroup having 1 to 20 carbon atoms, a substituted or unsubstituted andlinear, branched or cyclic alkylsilyl group having 1 to 10 carbon atoms,a substituted or unsubstituted arylsilyl group having 6 to 30 carbonatoms, a substituted or unsubstituted aryl group having 6 to 30 ringcarbon atoms, or a substituted or unsubstituted heteroaryl group having2 to 10 ring carbon atoms; f′ is an integer of 1 to 4; g′ is an integerof 1 to 3; and h′ is an integer of 1 to
 5. 4. The compound of claim 1,wherein k is 1, and m+n+p+q is less than or equal to
 6. 5. The compoundof claim 1, wherein each of Y₁ to Y₂ independently represents a hydrogenatom or a phenyl group.
 6. The compound of claim 1, wherein: k is 1; L₁,L₂, L₃, L₅ and L₆ each independently represent a single bond, asubstituted or unsubstituted phenylene group, a substituted orunsubstituted biphenylene group, a substituted or unsubstitutedterphenylene group, or a substituted or unsubstituted fluorenylenegroup; and L₄ and L₇ each independently represent a single bond, asubstituted or unsubstituted phenylene group, a substituted orunsubstituted biphenylene group, or a substituted or unsubstitutedterphenylene group.
 7. The compound of claim 1, wherein m+n=1 or 2, andp+q=1 or
 2. 8. The compound of claim 1, wherein, Ar represents amonocyclic aromatic ring selected from the group consisting of asubstituted or unsubstituted benzene ring having 2 to 6 ring carbonatoms, a pyrazole ring, an imidazole ring, a triazole ring, a pyridinering, a pyrimidine ring, a pyridazine ring, a pyrazine ring, a triazinering and a thiophene ring.
 9. The compound of claim 1, wherein Ar is abenzene ring.
 10. The compound of claim 1, wherein: Fl₁ and Fl₂ areindependently represented by formula (5):

Y₃ and Y₄ each independently represent: a hydrogen atom; a deuteriumatom; a linear, branched or cyclic alkyl group having 1 to 10 carbonatoms; a linear, branched or cyclic haloalkyl group having 1 to 10carbon atoms; a linear, branched or cyclic alkylsilyl group having 1 to10 carbon atoms; a substituted or unsubstituted arylsilyl group having 6to 30 carbon atoms; a substituted or unsubstituted aryl group having 6to 30 ring carbon atoms; or substituted or unsubstituted heteroarylgroup having 2 to 10 ring carbon atoms; and Y₅, Y₆, Y₇, Y₈, Y₉, Y₁₀ andY₁₁ each independently represent: a hydrogen atom; a deuterium atom; afluorine atom; a chlorine atom; a bromine atom; an iodine atom; a cyanogroup; a linear, branched or cyclic alkyl group having 1 to 10 carbonatoms; a linear, branched or cyclic alkoxy group having 1 to 10 carbonatoms; a linear, branched or cyclic haloalkyl group having 1 to 10carbon atoms; a linear, branched or cyclic haloalkoxy group having 1 to10 carbon atoms; a linear, branched or cyclic alkylsilyl group having 1to 10 carbon atoms; a substituted or unsubstituted arylsilyl grouphaving 6 to 30 carbon atoms; a substituted or unsubstituted aryl grouphaving 6 to 30 ring carbon atoms; or a substituted or unsubstitutedheteroaryl group having 2 to 10 ring carbon atoms.
 11. The compound ofclaim 10, wherein Y₃ and Y₄ independently represent a linear alkyl grouphaving 1 to 10 carbon atoms or a phenyl group.
 12. The compound of claim11, wherein Y₃ and Y₄ are both a methyl group.
 13. The compound of claim1, wherein Cz₁ and Cz₂ are independently represented by formula (3a) orformula (4a):


14. The compound of claim 1, wherein Nr₁ is a pyrimidine ring.
 15. Anorganic-electroluminescence-device material, comprising the compound ofclaim
 1. 16. An organic electroluminescence device, comprising: acathode; an anode; and an organic thin-film layer situated between thecathode and the anode, such that the organic thin-film layer is formedout of one or more layers comprising an emitting layer, wherein at leastone layer of the organic thin-film layer comprises thefluorene-containing aromatic compound of claim
 1. 17. The o device ofclaim 16, wherein the emitting layer comprises the fluorene-containingaromatic compound as a host material.
 18. The device of claim 16,wherein the emitting layer further comprises a phosphorescent material.19. The device of claim 18, wherein the emitting layer comprises a hostmaterial and the phosphorescent material, and the phosphorescentmaterial is an ortho metalation of a complex of a metal atom selectedfrom the group consisting of iridium (Ir), osmium (Os) and platinum(Pt).
 20. The device of claim 16, wherein the organic thin-film layercomprises an electron injecting layer situated between the cathode andthe emitting layer, and the electron injecting layer comprising anitrogen-containing cyclic derivative.
 21. The device of claim 16,wherein the organic thin-film layer comprises an electron transportinglayer situated between the cathode and the emitting layer, and theelectron transporting layer comprising the fluorene-containing aromaticcompound.
 22. The o device of claim 16, wherein a reduction-causingdopant is added in an interfacial region between the cathode and theorganic thin-film layer.